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MEGA PTA BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K955886
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1996
Days to Decision
74 days
Submission Type
Summary

MEGA PTA BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K955886
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1996
Days to Decision
74 days
Submission Type
Summary